| Literature DB >> 18199529 |
Stephan L Brown1, Konjeti R Sekhar, Girish Rachakonda, Soumya Sasi, Michael L Freeman.
Abstract
The transcription factor nuclear factor erythroid-derived 2-related factor 2 (Nrf2) regulates induction of an extensive cellular stress response network when complexed with the cAMP-responsive element binding protein (CBP) at antioxidant response elements (ARE) located in the promoter region of target genes. Activating transcription factor 3 (ATF3) can repress Nrf2-mediated signaling in a manner that is not well understood. Here, we show that ATF3-mediated suppression is a consequence of direct ATF3-Nrf2 protein-protein interactions that result in displacement of CBP from the ARE. This work establishes ATF3 as a novel repressor of the Nrf2-directed stress response pathway.Entities:
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Year: 2008 PMID: 18199529 DOI: 10.1158/0008-5472.CAN-07-2170
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701